Cas 108201-29-2,2-Ethoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin

108201-29-2

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Basic information

Product Name: 2-Ethoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin
Synonyms: 2-Ethoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin
CAS NO:108201-29-2
Molecular Formula:
Molecular Weight: 389.538
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-Ethoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin(CAS DataBase Reference)
NIST Chemistry Reference: 2-Ethoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin(108201-29-2)
EPA Substance Registry System: 2-Ethoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin(108201-29-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 108201-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 108201-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,2,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108201-29:
(8*1)+(7*0)+(6*8)+(5*2)+(4*0)+(3*1)+(2*2)+(1*9)=82
82 % 10 = 2
So 108201-29-2 is a valid CAS Registry Number.

108201-29-2Upstream product

108201-29-2Downstream Products

108201-28-1 2-Methoxy-9,9a-tetramethylen-3,4-diphenyl-7,8,9,9a-tetrahydro-2H,6H-pyrido<2.1-b><1.3>oxazin

108201-29-2Relevant academic research and scientific papers

Reactions of Cyclopropenones with Azomethines, VIII. Diphenylcyclopropenone and Cyclic Imines

Eicher, Theophil,Krause, Detlef

, p. 899 - 907 (2007/10/02)

Reactions of diphenylcyclopropenone (1a) and diphenyl cyclopropenethione (1b) with a variety of cyclic imines (derivatives of 3,4-dihydroisoquinolines 2-4, 2-substituted 1-pyrrolines 5 and 1-piperidines 6,7) gave rise to 2-pyrroline-4-ones and -4-thiones

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